N-Allyl-N,N-bis(trimethylsilyl)amine

95%

Reagent Code: #218570
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CAS Number 7688-51-9

science Other reagents with same CAS 7688-51-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.46 g/mol
Formula C₉H₂₃NSi₂
badge Registry Numbers
MDL Number MFCD00545193
thermostat Physical Properties
Boiling Point 72 °C at 15 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.816 g/mL at 25°C(lit.)
Storage 2-8°C

description Product Description

Used as a versatile reagent in organic synthesis, particularly in the preparation of allylsilanes and other silicon-containing compounds. It serves as a source of the N-allyl-bis(trimethylsilyl)amine anion, which can participate in nucleophilic reactions with electrophiles, enabling carbon–carbon bond formation. Its silyl groups enhance the stability and reactivity of intermediates in various transformations, including silylation and deprotonation processes. Commonly employed in the synthesis of complex molecules where controlled allylation is required, especially in pharmaceutical and agrochemical research. Also useful in the generation of enamines and iminium ions under mild conditions, making it valuable in catalytic and asymmetric synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,650.00
5g
10-20 days ฿6,650.00
25g
10-20 days ฿26,900.00
N-Allyl-N,N-bis(trimethylsilyl)amine
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Used as a versatile reagent in organic synthesis, particularly in the preparation of allylsilanes and other silicon-containing compounds. It serves as a source of the N-allyl-bis(trimethylsilyl)amine anion, which can participate in nucleophilic reactions with electrophiles, enabling carbon–carbon bond formation. Its silyl groups enhance the stability and reactivity of intermediates in various transformations, including silylation and deprotonation processes. Commonly employed in the synthesis of complex

Used as a versatile reagent in organic synthesis, particularly in the preparation of allylsilanes and other silicon-containing compounds. It serves as a source of the N-allyl-bis(trimethylsilyl)amine anion, which can participate in nucleophilic reactions with electrophiles, enabling carbon–carbon bond formation. Its silyl groups enhance the stability and reactivity of intermediates in various transformations, including silylation and deprotonation processes. Commonly employed in the synthesis of complex molecules where controlled allylation is required, especially in pharmaceutical and agrochemical research. Also useful in the generation of enamines and iminium ions under mild conditions, making it valuable in catalytic and asymmetric synthesis.

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